ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.448_451del (p.Ser150fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV004813327 SCV005438138 pathogenic Leber congenital amaurosis 10 2024-12-17 criteria provided, single submitter clinical testing

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